The present invention relates to a reflective contact for a III-nitride light emitting device.
Semiconductor light-emitting devices including light emitting diodes (LEDs), resonant cavity light emitting diodes (RCLEDs), vertical cavity laser diodes (VCSELs), and edge emitting lasers are among the most efficient light sources currently available. Materials systems currently of interest in the manufacture of high-brightness light emitting devices capable of operation across the visible spectrum include Group III-V semiconductors, particularly binary, ternary, and quaternary alloys of gallium, aluminum, indium, and nitrogen, also referred to as III-nitride materials. Typically, III-nitride light emitting devices are fabricated by epitaxially growing a stack of semiconductor layers of different compositions and dopant concentrations on a sapphire, silicon carbide, III-nitride, composite, or other suitable substrate by metal-organic chemical vapor deposition (MOCVD), molecular beam epitaxy (MBE), or other epitaxial techniques. The stack often includes one or more n-type layers doped with, for example, Si, formed over the substrate, one or more light emitting layers in an active region formed over the n-type layer or layers, and one or more p-type layers doped with, for example, Mg, formed over the active region. Electrical contacts are formed on the n- and p-type regions. III-nitride devices are often formed as inverted or flip chip devices, where both the n- and p-contacts formed on the same side of the semiconductor structure, and light is extracted from the side of the semiconductor structure opposite the contacts.
U.S. Pat. No. 6,514,782 describes III-nitride flip chip LEDs. “Because of the high resistivity of p-type III-nitride layers, LED designs employ metallization along the p-type layers to provide p-side current spreading . . . . For an inverted design, using highly reflective electrode metallizations is critical to improve the extraction efficiency . . . . The p electrode is the dominant factor for light extraction because it extends almost completely across the active area to provide uniform current injection into the p-n junction.
“The combination of low optical absorption and low contact resistivity in a manufacturable process are difficult to achieve for III-nitride devices. For example, Ag makes a good p-type Ohmic contact and is very reflective, but suffers from poor adhesion to III-nitride layers and from susceptibility to electro-migration in humid environments which can lead to catastrophic device failure. Al is reasonably reflective but does not make good Ohmic contact to p-type III-nitride materials, while other elemental metals are fairly absorbing (>25% absorption per pass in the visible wavelength regime). A possible solution is to use a multi-layer contact which includes a very thin semi-transparent Ohmic contact in conjunction with a thick reflective layer which acts as a current spreading layer. An optional barrier layer is included between the Ohmic layer and the reflective layer. One example of a p-type multi-layer contact is Au/NiOx/Al. Typical thicknesses for this metallization scheme are 30/100/1500 Å, Similarly, a suitable n-type GaN multi-layer contact is Ti/Al with typical thicknesses of 30/1500 Å, Since the p-electrode reflectivity is a dominant factor in extraction efficiency, it must not be compromised in designing for manufacturability.”
It is an object of the present invention to include in a reflective contact a thin, transparent current spreading layer and a transparent insulating material. In some embodiments, reflectivity of the contact may be improved over a device with a reflective metal contact.
Embodiments of the invention include a semiconductor structure comprising a III-nitride light emitting layer disposed between an n-type region and a p-type region. A contact disposed on the p-type region includes a transparent conductive material in direct contact with the p-type region, a reflective metal layer, and a transparent insulating material disposed between the transparent conductive layer and the reflective metal layer. In a plurality of openings in the transparent insulating material, the transparent conductive material is in direct contact with the reflective metal layer.
The performance of an LED may be improved by reducing optical loss associated with the p-contact, without increasing the forward voltage Vf required to forward bias the LED. A contact including a dielectric layer, which reflects by total internal reflection, may be more reflective than a contact where the sole reflective material is a metal reflector, such as the contacts described above in U.S. Pat. No. 6,514,782.
A conductive dielectric layer such as indium tin oxide (ITO) may be disposed between the p-type material and the silver p-contact. In such a bilayer, the ITO need not contribute to current spreading and the thickness may be optimized for highest reflectance; for example, the ITO may be 200 nm thick. However, ITO has an index of refraction higher than optimum for optical reflectivity and may absorb a significant amount of light at thicknesses required for high conductivity.
Alternatively, a nonconductive dielectric such as SiO2 may be disposed between the p-type material and the silver p-contact. Openings must be formed in the nonconductive dielectric to electrically connect the silver to the p-type material. The openings must be spaced close enough together to prevent current crowding in the poorly conductive p-type material. For example, the openings may be sub-micron size, which may require expensive and difficult techniques such as holographic or e-beam exposure of resist, or the use of a nano-imprinting tool. In addition, etching openings in the dielectric may damage the exposed p-type material, which may reduce the efficiency of an Ohmic contact formed on the damaged material.
In embodiments of the invention, the p-contact of a III-nitride LED includes three layers: a thin conductive layer in direct contact with the p-type semiconductor, a low-optical-loss dielectric layer disposed over the thin conductive layer with openings to facilitate electrical contact, and a reflective metal layer over the transparent dielectric layer.
A light emitting or active region 24 is grown over n-type region 22. Examples of suitable light emitting regions include a single thick or thin light emitting layer, or a multiple quantum well light emitting region including multiple thin or thick quantum well light emitting layers separated by barrier layers. For example, a multiple quantum well light emitting region may include multiple light emitting layers, each with a thickness of 25 Å or less, separated by barriers, each with a thickness of 100 Å or less. In some embodiments, the thickness of each of the light emitting layers in the device is thicker than 50 Å.
A p-type region 26 is grown over light emitting region 24. Like the n-type region, the p-type region may include multiple layers of different composition, thickness, and dopant concentration, including layers that are not intentionally doped, or n-type layers.
A thin conductive layer 28 is formed over p-type region 26. Thin conductive layer 28 may be, for example, silver, aluminum, or a conductive dielectric such as ITO, nickel oxide, ZnO or any other suitable semitransparent conductive material. A silver conductive layer 28 may be, for example, between 0.5 and 2 nm thick in some embodiments, between 2 and 8 nm thick in some embodiments, and 10 nm thick in some embodiments. A conductive layer 28 that is a transparent conductive oxide may be thicker. For example, the resistivity of an ITO conductive layer 28 may be 100 times greater than silver, requiring an ITO conductive layer 28 that is 100 times thicker than a silver conductive layer 28. To spread current several microns may require, for example, an ITO conductive layer 28 that is 200 nm thick. The material and thickness of conductive layer 28 may be selected such that current spreads in conductive layer 28 for 10 microns, for example.
In some embodiments, thin conductive layer 28 is formed as a group of small regions, rather than as a single, uninterrupted, continuous layer. In some embodiments, a thin layer of silver is evaporated on the surface of the p-type region 26, then annealed. During the anneal, the silver tends to agglomerate from a continuous, planar layer into a network of thicker, discrete regions, such as regions 50 in
A low optical loss material 30 is formed over conductive layer 28, Low-loss material 30 may be, for example, SiOx, SiNx, MgF2, Al2O3, or any other suitable highly transparent dielectric that is reflective, manufacturable, and readily adheres to the conductive layer 28. In some embodiments, low-loss material 30 has a low index of refraction, so the change in index of refraction between the low-loss material and the conductive layer 28 and p-type region 26 is as large as possible. Low-loss material 30 may be, for example, between 200 and 500 nm thick in some embodiments, between 250 and 350 nm thick in some embodiments, and 250 nm thick in some embodiments.
Openings 32 are then formed in the low-loss material 30, for example by conventional masking and etching steps. In some embodiments, endpoint detection is used to avoid etching the underlying conductive layer 28. In some embodiments, the low-loss material 30 is etched to near the endpoint with a dry etch, then a wet etch is used to etch the remaining thickness.
The size and spacing of the openings may be related to the resistivity and thickness of conductive layer 28. For example, a 150 nm thick layer of ITO has about the same sheet resistance as a 2 micron thick layer of n-GaN. In a device with a conventional contact formed on n-GaN, nearest neighbor n-contacts may be spaced about 150 microns apart. Accordingly, in a device according to embodiments of the invention with a 150 nm thick ITO conductive layer 28, the distance between openings 32 may be 150 microns. In a device according to embodiments of the invention with a 30 nm thick ITO conductive layer 28, the distance between openings 32 may be 30 microns. If the openings 32 are 3 microns in diameter spaced 30 microns apart, the surface coverage of openings 32 is about 1%.
The thickness of conductive layer 28 and low-loss material 30 depend on the individual materials used, as well as on the combination of materials.
A reflective conductive layer 34 is formed over the remaining low-loss material 30 and openings 32. Reflective layer 34 electrically connects to the p-type region 26 through openings 32 and conductive layer 28. Reflective layer 34 may be, for example, silver. Reflective layer 34 may be a multi-layer stack and may include, for example, one or more reflective metals, on or more Ohmic contact metals, and one or more guard metals or other guard materials. One example of a reflective layer 34 is a stack of silver, nickel, silver, then a guard metal such as TiWN, which may prevent or reduce electromigration of the silver.
The light extraction and hence performance of the LED may be improved by adding lossless scattering to the contact. In some embodiments, p-type region 26 is grown under conditions which create a rough surface, which may improve scattering over a smooth surface. Conductive layer 28 may be formed over the rough surface as a conformal layer, which would therefore also have a rough surface. A transparent low-loss layer 30 is then formed, for example by spin-coating, to cover the roughness and create a smooth surface. Openings are formed in the low-loss material and a reflective layer 34 is then formed, as described above. The roughness of the p-type region 26/conductive layer 28 interface may cause increased loss as compared to a smooth interface, but increased extraction may result in an overall improved performance. In some embodiments, scattering is increased by making low-loss layer 30 and/or conductive layer 28 porous or columnar in structure, for example by forming an ITO conductive layer 28 and/or a SiOx low-loss layer by oblique-angle deposition. The increase in porosity is accompanied by a reduction in refractive index which increases the reflectance of the contact. The porosity may be controlled by controlling the deposition angle, as described in “Quantification of porosity and deposition rate of nanoporous films grown by oblique-angle deposition,” Applied Physics Letters 93, 101914 (2008), which is incorporated herein by reference.
In one example, an Al-doped ZnO conductive layer 28 is applied to a rough p-type GaN layer grown as the top layer of the p-type region 26. A low index SiOx layer 30 is spin-coated over the ZnO to provide scattering at the ZnO/SiOx interface and to planarize the rough ZnO layer. Openings 32 are formed, then a silver reflective layer 34 is deposited.
In some embodiments, low-loss material 30 is a multi-layer dielectric stack. The layers closest to the conductive layer 28 and the reflective layer 34 are chosen for good adhesion. The inner layers are chosen for minimum refractive index. Multiple layers may be formed, for example, in a single processing step. A multi-layer low-loss structure 30 may be more reliable and more reflective than a single layer. In addition, the difference in index of refraction between the layers in a multi-layer stack may provide scattering, particularly when a multi-layer stack is applied to a rough surface, as described above.
In some embodiments, the etch depth of the openings 32 in the low-loss material 30 is increased to include removal of some of the underlying conductive layer 28, as illustrated in
LED 42 is bonded to mount 40 by n- and p-interconnects 56 and 58. Interconnects 56 and 58 may be any suitable material, such as solder or other metals, and may include multiple layers of materials. In some embodiments, interconnects include at least one gold layer and the bond between LED 42 and mount 40 is formed by ultrasonic bonding.
During ultrasonic bonding, the LED die 42 is positioned on a mount 40. A bond head is positioned on the top surface of the LED die, often the top surface of a sapphire growth substrate in the case of a III-nitride device grown on sapphire. The bond head is connected to an ultrasonic transducer. The ultrasonic transducer may be, for example, a stack of lead zirconate titanate (PZT) layers. When a voltage is applied to the transducer at a frequency that causes the system to resonate harmonically (often a frequency on the order of tens or hundreds of kHz), the transducer begins to vibrate, which in turn causes the bond head and the LED die to vibrate, often at an amplitude on the order of microns. The vibration causes atoms in the metal lattice of a structure on the LED 42 to interdiffuse with a structure on mount 40, resulting in a metallurgically continuous joint. Heat and/or pressure may be added during bonding.
After bonding LED die 42 to mount 40, the growth substrate on which the semiconductor layers were grown may be removed, for example by laser lift off, etching, or any other technique suitable to a particular growth substrate. After removing the growth substrate, the semiconductor structure may be thinned, for example by photoelectrochemical etching, and/or the surface may be roughened or patterned, for example with a photonic crystal structure. A lens, wavelength converting material, or other structure known in the art may be disposed over LED 42 after substrate removal.
Having described the invention in detail, those skilled in the art will appreciate that, given the present disclosure, modifications may be made to the invention without departing from the spirit of the inventive concept described herein. Therefore, it is not intended that the scope of the invention be limited to the specific embodiments illustrated and described.
This application is a Divisional of U.S. patent application Ser. No. 12/491,976, filed 25 Jun. 2009.
Number | Name | Date | Kind |
---|---|---|---|
5045408 | Williams | Sep 1991 | A |
5272108 | Kozawa | Dec 1993 | A |
5917202 | Haitz et al. | Jun 1999 | A |
6008539 | Shibata | Dec 1999 | A |
6194743 | Kondoh et al. | Feb 2001 | B1 |
6291839 | Lester | Sep 2001 | B1 |
6291840 | Uemura | Sep 2001 | B1 |
6303405 | Yoshida | Oct 2001 | B1 |
6420732 | Kung | Jul 2002 | B1 |
6441403 | Chang | Aug 2002 | B1 |
6465808 | Lin | Oct 2002 | B2 |
6512248 | Takeuchi | Jan 2003 | B1 |
6514782 | Wierer, Jr. et al. | Feb 2003 | B1 |
6547249 | Collins, III | Apr 2003 | B2 |
6576488 | Collins, III | Jun 2003 | B2 |
6657236 | Thibeault | Dec 2003 | B1 |
6693352 | Huang | Feb 2004 | B1 |
6748001 | Nishitsuka | Jun 2004 | B1 |
6784010 | Yamaguchi | Aug 2004 | B2 |
6784462 | Schubert | Aug 2004 | B2 |
6794690 | Uemura | Sep 2004 | B2 |
6797987 | Chen | Sep 2004 | B2 |
6891197 | Bhat | May 2005 | B2 |
6916676 | Sano | Jul 2005 | B2 |
6946372 | Kim | Sep 2005 | B2 |
6946685 | Steigerwald | Sep 2005 | B1 |
6990132 | Kneissl | Jan 2006 | B2 |
6998649 | Hata | Feb 2006 | B2 |
7009218 | Sugimoto | Mar 2006 | B2 |
7064354 | Chen | Jun 2006 | B2 |
7072374 | Matsumura | Jul 2006 | B2 |
7166483 | Liu | Jan 2007 | B2 |
7173311 | Sato | Feb 2007 | B2 |
7279751 | Ueda | Oct 2007 | B2 |
7291865 | Kojima | Nov 2007 | B2 |
7294864 | Kim | Nov 2007 | B2 |
7326967 | Hsieh et al. | Feb 2008 | B2 |
7335916 | Kim et al. | Feb 2008 | B2 |
7375380 | Asahara et al. | May 2008 | B2 |
7406111 | Sung | Jul 2008 | B2 |
7491979 | Kwak | Feb 2009 | B2 |
7501665 | Yasuda | Mar 2009 | B2 |
7512167 | Izu | Mar 2009 | B2 |
7557379 | Haberern | Jul 2009 | B2 |
7569432 | Chang | Aug 2009 | B1 |
7576367 | Sugimori | Aug 2009 | B2 |
7592637 | Zimmerman | Sep 2009 | B2 |
7646036 | Kozawa | Jan 2010 | B2 |
7646798 | Michiue | Jan 2010 | B2 |
7659553 | Kato et al. | Feb 2010 | B2 |
7679097 | Akaishi | Mar 2010 | B2 |
7683381 | Hsu et al. | Mar 2010 | B2 |
7687323 | Matsuo et al. | Mar 2010 | B2 |
7724321 | Hsieh | May 2010 | B2 |
7732231 | Aldaz | Jun 2010 | B1 |
7738524 | Ochiai | Jun 2010 | B2 |
7755095 | Nagai | Jul 2010 | B2 |
7781791 | Sakai et al. | Aug 2010 | B2 |
7791101 | Bergmann | Sep 2010 | B2 |
7847312 | Fudeta | Dec 2010 | B2 |
7867885 | Bae | Jan 2011 | B2 |
7871840 | Nomaguchi | Jan 2011 | B2 |
7902565 | Katsuno | Mar 2011 | B2 |
7915629 | Li et al. | Mar 2011 | B2 |
7915636 | Lee | Mar 2011 | B2 |
7922939 | Lewis | Apr 2011 | B2 |
7935554 | Lee | May 2011 | B2 |
7952106 | Hsu | May 2011 | B2 |
7973325 | Kim et al. | Jul 2011 | B2 |
7981704 | Abe | Jul 2011 | B2 |
7982236 | Sano et al. | Jul 2011 | B2 |
7985979 | David | Jul 2011 | B2 |
7989820 | Lee | Aug 2011 | B2 |
8017970 | Katsuno | Sep 2011 | B2 |
8093608 | Muramoto | Jan 2012 | B2 |
8101964 | Kitagawa | Jan 2012 | B2 |
8115222 | Matsui | Feb 2012 | B2 |
8120049 | Matsuo | Feb 2012 | B2 |
8129743 | Suehiro | Mar 2012 | B2 |
8138518 | Tsai | Mar 2012 | B2 |
8143643 | Choo | Mar 2012 | B2 |
8168966 | Biwa et al. | May 2012 | B2 |
8174037 | Edmond et al. | May 2012 | B2 |
8247837 | Lin | Aug 2012 | B2 |
8368100 | Donofrio | Feb 2013 | B2 |
8378376 | Chung | Feb 2013 | B2 |
8525129 | Offermans | Sep 2013 | B2 |
8525204 | Fukshima et al. | Sep 2013 | B2 |
8526476 | Engl | Sep 2013 | B2 |
8530923 | Sabathil et al. | Sep 2013 | B2 |
8679869 | Aldaz | Mar 2014 | B2 |
9070837 | Katsuno | Jun 2015 | B2 |
9246073 | Sasaoka | Jan 2016 | B2 |
9508902 | Ko | Nov 2016 | B2 |
20020014630 | Okazaki | Feb 2002 | A1 |
20030146445 | Hen | Aug 2003 | A1 |
20040026702 | Yamada | Feb 2004 | A1 |
20040038519 | Yanagisawa et al. | Feb 2004 | A1 |
20050067625 | Hata | Mar 2005 | A1 |
20050072968 | Tsai | Apr 2005 | A1 |
20050121685 | Seong | Jun 2005 | A1 |
20050156183 | Tsai | Jul 2005 | A1 |
20050199895 | Seong | Sep 2005 | A1 |
20060011925 | Bader et al. | Jan 2006 | A1 |
20060046328 | Raffetto et al. | Mar 2006 | A1 |
20060127567 | Uehara et al. | Jun 2006 | A1 |
20060154389 | Doan | Jul 2006 | A1 |
20060192223 | Lee | Aug 2006 | A1 |
20060273335 | Asahara | Dec 2006 | A1 |
20060273336 | Fujikura | Dec 2006 | A1 |
20060289886 | Sakai | Dec 2006 | A1 |
20070096130 | Schiaffino | May 2007 | A1 |
20070102692 | Asahara et al. | May 2007 | A1 |
20070145380 | Shum | Jun 2007 | A1 |
20080048202 | Tazima | Feb 2008 | A1 |
20080048206 | Lee | Feb 2008 | A1 |
20080068821 | Wang et al. | Mar 2008 | A1 |
20080185606 | Sano et al. | Aug 2008 | A1 |
20080296602 | Liu | Dec 2008 | A1 |
20080308832 | Hsieh | Dec 2008 | A1 |
20090134418 | Lee | May 2009 | A1 |
20100051978 | Katsuno | Mar 2010 | A1 |
20100148190 | Kim et al. | Jun 2010 | A1 |
20110140152 | Song | Jun 2011 | A1 |
Number | Date | Country |
---|---|---|
1677703 | Mar 2005 | CN |
1877874 | Dec 2006 | CN |
101213678 | Jul 2008 | CN |
101355119 | Jan 2009 | CN |
102008035900 | Nov 2009 | DE |
7131070 | May 1995 | JP |
09167859 | Jun 1997 | JP |
10209500 | Aug 1998 | JP |
11186599 | Jul 1999 | JP |
2002016286 | Jan 2002 | JP |
2003224297 | Aug 2003 | JP |
2005191219 | Jul 2005 | JP |
2005197289 | Jul 2005 | JP |
2006093358 | Apr 2006 | JP |
2007013045 | Jan 2007 | JP |
2008010608 | Jan 2008 | JP |
2009088299 | Apr 2009 | JP |
2009260316 | Nov 2009 | JP |
2006006555 | Jan 2006 | WO |
2006006822 | Jan 2006 | WO |
2007004701 | Jan 2007 | WO |
2009010762 | Jan 2009 | WO |
Entry |
---|
Yamada et al., “InGaN-Based Near-Ultraviolet and Blue-Light-Emitting Diodes with High External Quantum Efficiency Using a Patterned Sapphire Substrate with a Mesh Electrode”, Japanese Journal of Applied Physics 41 (2002) pp. L1431-L1433. |
Kim et al., “High-Reflectivity Al—Pt Nanostructured Ohmic Contact to p-GaN,” IEEE Transactions On Electron Devices 53 Oct. 2006 pp. 2448-2453. |
Kim Hyunsoo et al. , “Light Extraction Enhancement of GaN-based Light Emitting Diodes using MgF2/Al Omnidirectional Reflectors” Journal of Applied Physics 104, 053111(2008) p. 1-4. |
D.J. Poxson et al., “Quantification of Porosity and Deposition Rate of Nanoporous Films Grown by Oblique Angle Deposition”, Applied Journal of Physics Letters, 93, 101914 2008, p. 1-3. |
EP Office Action for Application No. 10726287.5, dated Oct. 23, 2015, 5 pages. |
First Office Action and Search Report for CN Application No. 201080028617.4, dated Aug. 6, 2014, 22 pages. |
JP Office Action for Application No. 2012-516887, dated May 28, 2015, 14 pages. |
Second Office Action for CN Application No. 201080028617.4, dated Mar. 17, 2015, 11 pages. |
Third Office Action for CN Application No. 201080028617.4, dated Nov. 4, 2015, 13 pages. |
TW Office Action for Application No. 099116193, dated Nov. 27, 2015, 9 pages. |
WO International Search Report and Written Opinion dated Dec. 14, 2010, 12 pages. |
10-2012-7001895 KR OA, Jan. 13, 2016, 10 pps. |
JP Office Action, Application 2015-187919, dated Jun. 21, 2016, 5 pps. |
KR Office Action, Application No. 10-2012-7001895, dated Jul. 30, 2016. |
TW Office Action, Application 099116193, dated Jul. 6, 2016, 5 pps. |
JP Office Action, Application 2015-187919, dated Jan. 17, 2017, 6 pps. |
Number | Date | Country | |
---|---|---|---|
20120199863 A1 | Aug 2012 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 12491976 | Jun 2009 | US |
Child | 13448700 | US |